Carries an ATP pyrophosphate-lyase domain on its cytoplasmic segment. Likely acts as a receptor for some unknown extracellular stimulus. Extremely expanded kinetoplastid protein family.. Expressed in the insect stage (promastigote) but not in the mammalian host stage of the parasite life cycle.. Localization: Cell surface (by feature)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 57 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 45, no: 26 |
NetGPI | no | yes: 0, no: 71 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 66 |
GO:0110165 | cellular anatomical entity | 1 | 72 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 72 |
GO:0006163 | purine nucleotide metabolic process | 5 | 72 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 72 |
GO:0006171 | cAMP biosynthetic process | 8 | 72 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 72 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 72 |
GO:0006793 | phosphorus metabolic process | 3 | 72 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 72 |
GO:0006807 | nitrogen compound metabolic process | 2 | 72 |
GO:0007165 | signal transduction | 2 | 72 |
GO:0008152 | metabolic process | 1 | 72 |
GO:0009058 | biosynthetic process | 2 | 72 |
GO:0009117 | nucleotide metabolic process | 5 | 72 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 72 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 72 |
GO:0009165 | nucleotide biosynthetic process | 6 | 72 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 72 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 72 |
GO:0009259 | ribonucleotide metabolic process | 5 | 72 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 72 |
GO:0009987 | cellular process | 1 | 72 |
GO:0018130 | heterocycle biosynthetic process | 4 | 72 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 72 |
GO:0019637 | organophosphate metabolic process | 3 | 72 |
GO:0019693 | ribose phosphate metabolic process | 4 | 72 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 72 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 72 |
GO:0035556 | intracellular signal transduction | 3 | 72 |
GO:0044237 | cellular metabolic process | 2 | 72 |
GO:0044238 | primary metabolic process | 2 | 72 |
GO:0044249 | cellular biosynthetic process | 3 | 72 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 72 |
GO:0044281 | small molecule metabolic process | 2 | 72 |
GO:0046058 | cAMP metabolic process | 7 | 72 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 72 |
GO:0046483 | heterocycle metabolic process | 3 | 72 |
GO:0050789 | regulation of biological process | 2 | 72 |
GO:0050794 | regulation of cellular process | 3 | 72 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 72 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 72 |
GO:0065007 | biological regulation | 1 | 72 |
GO:0071704 | organic substance metabolic process | 2 | 72 |
GO:0072521 | purine-containing compound metabolic process | 4 | 72 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 72 |
GO:0090407 | organophosphate biosynthetic process | 4 | 72 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 72 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 72 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 72 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 72 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 72 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 72 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 72 |
GO:1901576 | organic substance biosynthetic process | 3 | 72 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 61 |
GO:0016829 | lyase activity | 2 | 61 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1156 | 1160 | PF00656 | 0.465 |
CLV_C14_Caspase3-7 | 1194 | 1198 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.387 |
CLV_C14_Caspase3-7 | 852 | 856 | PF00656 | 0.629 |
CLV_C14_Caspase3-7 | 913 | 917 | PF00656 | 0.509 |
CLV_MEL_PAP_1 | 428 | 434 | PF00089 | 0.431 |
CLV_NRD_NRD_1 | 1236 | 1238 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.550 |
CLV_PCSK_KEX2_1 | 1234 | 1236 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 1325 | 1327 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 1234 | 1236 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 1325 | 1327 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 1049 | 1053 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 1066 | 1070 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 1136 | 1140 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 1152 | 1156 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 1281 | 1285 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 1326 | 1330 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 725 | 729 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 865 | 869 | PF00082 | 0.263 |
DEG_APCC_DBOX_1 | 724 | 732 | PF00400 | 0.392 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.558 |
DEG_ODPH_VHL_1 | 1091 | 1103 | PF01847 | 0.523 |
DEG_SCF_FBW7_1 | 1294 | 1301 | PF00400 | 0.401 |
DEG_SCF_FBW7_1 | 819 | 824 | PF00400 | 0.287 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.277 |
DEG_SPOP_SBC_1 | 599 | 603 | PF00917 | 0.454 |
DOC_ANK_TNKS_1 | 1207 | 1214 | PF00023 | 0.514 |
DOC_CKS1_1 | 1109 | 1114 | PF01111 | 0.517 |
DOC_CYCLIN_RxL_1 | 1133 | 1141 | PF00134 | 0.452 |
DOC_CYCLIN_yCln2_LP_2 | 1374 | 1377 | PF00134 | 0.401 |
DOC_CYCLIN_yCln2_LP_2 | 515 | 521 | PF00134 | 0.467 |
DOC_MAPK_FxFP_2 | 234 | 237 | PF00069 | 0.260 |
DOC_MAPK_gen_1 | 1234 | 1241 | PF00069 | 0.742 |
DOC_MAPK_gen_1 | 1392 | 1400 | PF00069 | 0.401 |
DOC_MAPK_JIP1_4 | 865 | 871 | PF00069 | 0.401 |
DOC_PP1_RVXF_1 | 662 | 668 | PF00149 | 0.355 |
DOC_PP2B_LxvP_1 | 1373 | 1376 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 259 | 262 | PF13499 | 0.251 |
DOC_PP2B_LxvP_1 | 29 | 32 | PF13499 | 0.374 |
DOC_PP4_FxxP_1 | 234 | 237 | PF00568 | 0.303 |
DOC_PP4_FxxP_1 | 520 | 523 | PF00568 | 0.308 |
DOC_USP7_MATH_1 | 1079 | 1083 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.283 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 720 | 724 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 952 | 956 | PF00917 | 0.609 |
DOC_USP7_MATH_2 | 1244 | 1250 | PF00917 | 0.523 |
DOC_USP7_MATH_2 | 477 | 483 | PF00917 | 0.250 |
DOC_USP7_UBL2_3 | 1136 | 1140 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 861 | 865 | PF12436 | 0.401 |
DOC_WW_Pin1_4 | 1108 | 1113 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 1124 | 1129 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 1224 | 1229 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 1294 | 1299 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 696 | 701 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 815 | 820 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 961 | 966 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 968 | 973 | PF00397 | 0.435 |
LIG_14-3-3_CanoR_1 | 1049 | 1054 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 1066 | 1075 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 1152 | 1162 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 1172 | 1180 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 1216 | 1221 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 1346 | 1351 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 1394 | 1400 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 249 | 256 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 710 | 715 | PF00244 | 0.378 |
LIG_Actin_WH2_2 | 1034 | 1051 | PF00022 | 0.592 |
LIG_AP2alpha_1 | 222 | 226 | PF02296 | 0.212 |
LIG_APCC_ABBA_1 | 637 | 642 | PF00400 | 0.332 |
LIG_APCC_ABBA_1 | 987 | 992 | PF00400 | 0.598 |
LIG_BIR_III_2 | 1209 | 1213 | PF00653 | 0.695 |
LIG_BRCT_BRCA1_1 | 1064 | 1068 | PF00533 | 0.577 |
LIG_BRCT_BRCA1_1 | 1217 | 1221 | PF00533 | 0.666 |
LIG_BRCT_BRCA1_1 | 1305 | 1309 | PF00533 | 0.609 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.371 |
LIG_BRCT_BRCA1_1 | 466 | 470 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 601 | 605 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_1 | 684 | 688 | PF00533 | 0.309 |
LIG_CSL_BTD_1 | 88 | 91 | PF09270 | 0.350 |
LIG_eIF4E_1 | 1369 | 1375 | PF01652 | 0.564 |
LIG_FHA_1 | 1009 | 1015 | PF00498 | 0.513 |
LIG_FHA_1 | 1021 | 1027 | PF00498 | 0.514 |
LIG_FHA_1 | 1050 | 1056 | PF00498 | 0.598 |
LIG_FHA_1 | 1171 | 1177 | PF00498 | 0.598 |
LIG_FHA_1 | 1190 | 1196 | PF00498 | 0.663 |
LIG_FHA_1 | 1236 | 1242 | PF00498 | 0.613 |
LIG_FHA_1 | 1255 | 1261 | PF00498 | 0.656 |
LIG_FHA_1 | 1289 | 1295 | PF00498 | 0.640 |
LIG_FHA_1 | 1378 | 1384 | PF00498 | 0.615 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.347 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.336 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.513 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.503 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.386 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.325 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.357 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.377 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.348 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.291 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.432 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.427 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.413 |
LIG_FHA_1 | 762 | 768 | PF00498 | 0.484 |
LIG_FHA_1 | 802 | 808 | PF00498 | 0.383 |
LIG_FHA_1 | 818 | 824 | PF00498 | 0.454 |
LIG_FHA_1 | 825 | 831 | PF00498 | 0.348 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.431 |
LIG_FHA_2 | 1029 | 1035 | PF00498 | 0.597 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.348 |
LIG_FHA_2 | 1154 | 1160 | PF00498 | 0.501 |
LIG_FHA_2 | 1359 | 1365 | PF00498 | 0.444 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.489 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.397 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.475 |
LIG_FHA_2 | 870 | 876 | PF00498 | 0.509 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.363 |
LIG_FHA_2 | 911 | 917 | PF00498 | 0.513 |
LIG_FHA_2 | 945 | 951 | PF00498 | 0.509 |
LIG_GBD_Chelix_1 | 931 | 939 | PF00786 | 0.418 |
LIG_LIR_Apic_2 | 1123 | 1128 | PF02991 | 0.497 |
LIG_LIR_Apic_2 | 231 | 237 | PF02991 | 0.454 |
LIG_LIR_Apic_2 | 346 | 351 | PF02991 | 0.272 |
LIG_LIR_Apic_2 | 517 | 523 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 244 | 251 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 483 | 490 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 524 | 534 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 778 | 786 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 868 | 879 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 924 | 932 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 1037 | 1043 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 1123 | 1129 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 1324 | 1330 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 524 | 529 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 644 | 650 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 797 | 802 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 868 | 874 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 924 | 929 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 950 | 956 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 970 | 976 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 995 | 1001 | PF02991 | 0.486 |
LIG_NRBOX | 22 | 28 | PF00104 | 0.342 |
LIG_PCNA_yPIPBox_3 | 249 | 260 | PF02747 | 0.397 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.260 |
LIG_Pex14_2 | 358 | 362 | PF04695 | 0.468 |
LIG_Pex14_2 | 846 | 850 | PF04695 | 0.477 |
LIG_PTB_Apo_2 | 138 | 145 | PF02174 | 0.362 |
LIG_PTB_Apo_2 | 356 | 363 | PF02174 | 0.324 |
LIG_PTB_Phospho_1 | 138 | 144 | PF10480 | 0.278 |
LIG_Rb_LxCxE_1 | 916 | 938 | PF01857 | 0.401 |
LIG_Rb_pABgroove_1 | 392 | 400 | PF01858 | 0.215 |
LIG_Rb_pABgroove_1 | 634 | 642 | PF01858 | 0.334 |
LIG_SH2_CRK | 1001 | 1005 | PF00017 | 0.597 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.393 |
LIG_SH2_CRK | 526 | 530 | PF00017 | 0.247 |
LIG_SH2_CRK | 697 | 701 | PF00017 | 0.464 |
LIG_SH2_GRB2like | 1293 | 1296 | PF00017 | 0.518 |
LIG_SH2_GRB2like | 357 | 360 | PF00017 | 0.347 |
LIG_SH2_GRB2like | 526 | 529 | PF00017 | 0.262 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.353 |
LIG_SH2_PTP2 | 706 | 709 | PF00017 | 0.393 |
LIG_SH2_SRC | 1161 | 1164 | PF00017 | 0.653 |
LIG_SH2_SRC | 1293 | 1296 | PF00017 | 0.702 |
LIG_SH2_SRC | 526 | 529 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 1395 | 1399 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 189 | 193 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 732 | 736 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 779 | 783 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 1129 | 1132 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 732 | 735 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 1125 | 1128 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 1129 | 1132 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 1161 | 1164 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 1293 | 1296 | PF00017 | 0.668 |
LIG_SH2_STAT5 | 1341 | 1344 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 706 | 709 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 732 | 735 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 775 | 778 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 794 | 797 | PF00017 | 0.281 |
LIG_SH3_3 | 1039 | 1045 | PF00018 | 0.452 |
LIG_SH3_3 | 1048 | 1054 | PF00018 | 0.432 |
LIG_SH3_3 | 1222 | 1228 | PF00018 | 0.694 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.391 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.445 |
LIG_SUMO_SIM_anti_2 | 1256 | 1263 | PF11976 | 0.611 |
LIG_SUMO_SIM_anti_2 | 20 | 25 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 607 | 614 | PF11976 | 0.360 |
LIG_SUMO_SIM_anti_2 | 633 | 642 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 1165 | 1171 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 1237 | 1242 | PF11976 | 0.638 |
LIG_SUMO_SIM_par_1 | 1256 | 1263 | PF11976 | 0.621 |
LIG_SUMO_SIM_par_1 | 1266 | 1271 | PF11976 | 0.672 |
LIG_SUMO_SIM_par_1 | 387 | 393 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 607 | 614 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 633 | 642 | PF11976 | 0.421 |
LIG_TRAF2_1 | 1031 | 1034 | PF00917 | 0.538 |
LIG_TRAF2_1 | 1249 | 1252 | PF00917 | 0.690 |
LIG_TYR_ITIM | 441 | 446 | PF00017 | 0.468 |
LIG_TYR_ITSM | 522 | 529 | PF00017 | 0.219 |
LIG_UBA3_1 | 1315 | 1322 | PF00899 | 0.444 |
LIG_UBA3_1 | 390 | 396 | PF00899 | 0.436 |
LIG_UBA3_1 | 415 | 419 | PF00899 | 0.234 |
LIG_WRC_WIRS_1 | 1080 | 1085 | PF05994 | 0.468 |
LIG_WRC_WIRS_1 | 953 | 958 | PF05994 | 0.401 |
LIG_WW_3 | 1149 | 1153 | PF00397 | 0.660 |
MOD_CDK_SPK_2 | 817 | 822 | PF00069 | 0.309 |
MOD_CDK_SPxxK_3 | 815 | 822 | PF00069 | 0.383 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.383 |
MOD_CK1_1 | 1127 | 1133 | PF00069 | 0.519 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.290 |
MOD_CK1_1 | 1250 | 1256 | PF00069 | 0.711 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.355 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.434 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.324 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.319 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.301 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.375 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.421 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.399 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.426 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.418 |
MOD_CK1_1 | 699 | 705 | PF00069 | 0.346 |
MOD_CK1_1 | 755 | 761 | PF00069 | 0.413 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.428 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.469 |
MOD_CK1_1 | 971 | 977 | PF00069 | 0.565 |
MOD_CK2_1 | 1022 | 1028 | PF00069 | 0.532 |
MOD_CK2_1 | 1114 | 1120 | PF00069 | 0.534 |
MOD_CK2_1 | 1220 | 1226 | PF00069 | 0.560 |
MOD_CK2_1 | 1246 | 1252 | PF00069 | 0.629 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.446 |
MOD_CK2_1 | 1298 | 1304 | PF00069 | 0.448 |
MOD_CK2_1 | 1345 | 1351 | PF00069 | 0.416 |
MOD_CK2_1 | 1358 | 1364 | PF00069 | 0.458 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.407 |
MOD_CK2_1 | 657 | 663 | PF00069 | 0.454 |
MOD_CK2_1 | 809 | 815 | PF00069 | 0.508 |
MOD_CK2_1 | 869 | 875 | PF00069 | 0.510 |
MOD_CK2_1 | 961 | 967 | PF00069 | 0.526 |
MOD_GlcNHglycan | 1070 | 1073 | PF01048 | 0.394 |
MOD_GlcNHglycan | 1173 | 1176 | PF01048 | 0.372 |
MOD_GlcNHglycan | 1300 | 1303 | PF01048 | 0.413 |
MOD_GlcNHglycan | 1304 | 1308 | PF01048 | 0.408 |
MOD_GlcNHglycan | 1395 | 1398 | PF01048 | 0.425 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.621 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.596 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.615 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.575 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.524 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.610 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.631 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.507 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.507 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.592 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.622 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.561 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.544 |
MOD_GlcNHglycan | 771 | 774 | PF01048 | 0.572 |
MOD_GlcNHglycan | 811 | 814 | PF01048 | 0.773 |
MOD_GlcNHglycan | 93 | 97 | PF01048 | 0.699 |
MOD_GlcNHglycan | 973 | 976 | PF01048 | 0.318 |
MOD_GSK3_1 | 1004 | 1011 | PF00069 | 0.536 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.361 |
MOD_GSK3_1 | 1216 | 1223 | PF00069 | 0.609 |
MOD_GSK3_1 | 1246 | 1253 | PF00069 | 0.708 |
MOD_GSK3_1 | 1268 | 1275 | PF00069 | 0.736 |
MOD_GSK3_1 | 1294 | 1301 | PF00069 | 0.634 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.536 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.377 |
MOD_GSK3_1 | 1330 | 1337 | PF00069 | 0.625 |
MOD_GSK3_1 | 1358 | 1365 | PF00069 | 0.630 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.463 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.271 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.416 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.437 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.431 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.328 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.323 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.412 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.411 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.353 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.331 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.418 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.379 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.397 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.362 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.383 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.436 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.360 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.403 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.448 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.414 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.472 |
MOD_GSK3_1 | 865 | 872 | PF00069 | 0.522 |
MOD_GSK3_1 | 910 | 917 | PF00069 | 0.516 |
MOD_GSK3_1 | 957 | 964 | PF00069 | 0.628 |
MOD_GSK3_1 | 967 | 974 | PF00069 | 0.601 |
MOD_LATS_1 | 11 | 17 | PF00433 | 0.415 |
MOD_N-GLC_1 | 1294 | 1299 | PF02516 | 0.322 |
MOD_N-GLC_1 | 1330 | 1335 | PF02516 | 0.415 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.467 |
MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.633 |
MOD_N-GLC_1 | 808 | 813 | PF02516 | 0.672 |
MOD_N-GLC_2 | 10 | 12 | PF02516 | 0.544 |
MOD_N-GLC_2 | 42 | 44 | PF02516 | 0.414 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.422 |
MOD_NEK2_1 | 1068 | 1073 | PF00069 | 0.587 |
MOD_NEK2_1 | 1138 | 1143 | PF00069 | 0.537 |
MOD_NEK2_1 | 1165 | 1170 | PF00069 | 0.649 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.426 |
MOD_NEK2_1 | 1254 | 1259 | PF00069 | 0.589 |
MOD_NEK2_1 | 1268 | 1273 | PF00069 | 0.587 |
MOD_NEK2_1 | 1393 | 1398 | PF00069 | 0.401 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.421 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.315 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.272 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.321 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.419 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.426 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.444 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.368 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.368 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.382 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.318 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.467 |
MOD_NEK2_1 | 714 | 719 | PF00069 | 0.406 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.419 |
MOD_NEK2_1 | 880 | 885 | PF00069 | 0.555 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.326 |
MOD_NEK2_2 | 426 | 431 | PF00069 | 0.398 |
MOD_NEK2_2 | 584 | 589 | PF00069 | 0.484 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.485 |
MOD_PIKK_1 | 1247 | 1253 | PF00454 | 0.731 |
MOD_PIKK_1 | 1358 | 1364 | PF00454 | 0.444 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.379 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.383 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.419 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.496 |
MOD_PIKK_1 | 641 | 647 | PF00454 | 0.409 |
MOD_PIKK_1 | 730 | 736 | PF00454 | 0.364 |
MOD_PK_1 | 1010 | 1016 | PF00069 | 0.442 |
MOD_PK_1 | 1216 | 1222 | PF00069 | 0.709 |
MOD_PKA_1 | 1235 | 1241 | PF00069 | 0.735 |
MOD_PKA_2 | 1171 | 1177 | PF00069 | 0.609 |
MOD_PKA_2 | 1215 | 1221 | PF00069 | 0.656 |
MOD_PKA_2 | 1235 | 1241 | PF00069 | 0.744 |
MOD_PKA_2 | 1345 | 1351 | PF00069 | 0.453 |
MOD_PKA_2 | 1358 | 1364 | PF00069 | 0.460 |
MOD_PKA_2 | 1393 | 1399 | PF00069 | 0.401 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.391 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.417 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.413 |
MOD_Plk_1 | 1033 | 1039 | PF00069 | 0.571 |
MOD_Plk_1 | 1287 | 1293 | PF00069 | 0.633 |
MOD_Plk_1 | 1334 | 1340 | PF00069 | 0.618 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.378 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.487 |
MOD_Plk_1 | 527 | 533 | PF00069 | 0.339 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.382 |
MOD_Plk_1 | 641 | 647 | PF00069 | 0.385 |
MOD_Plk_1 | 679 | 685 | PF00069 | 0.449 |
MOD_Plk_1 | 740 | 746 | PF00069 | 0.415 |
MOD_Plk_2-3 | 1028 | 1034 | PF00069 | 0.425 |
MOD_Plk_2-3 | 1105 | 1111 | PF00069 | 0.665 |
MOD_Plk_2-3 | 310 | 316 | PF00069 | 0.441 |
MOD_Plk_2-3 | 910 | 916 | PF00069 | 0.509 |
MOD_Plk_4 | 1022 | 1028 | PF00069 | 0.486 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.369 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.357 |
MOD_Plk_4 | 1216 | 1222 | PF00069 | 0.722 |
MOD_Plk_4 | 1254 | 1260 | PF00069 | 0.709 |
MOD_Plk_4 | 1288 | 1294 | PF00069 | 0.687 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.419 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.368 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.405 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.375 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.414 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.270 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.343 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.374 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.389 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.429 |
MOD_Plk_4 | 710 | 716 | PF00069 | 0.354 |
MOD_Plk_4 | 821 | 827 | PF00069 | 0.353 |
MOD_Plk_4 | 865 | 871 | PF00069 | 0.509 |
MOD_Plk_4 | 914 | 920 | PF00069 | 0.520 |
MOD_Plk_4 | 944 | 950 | PF00069 | 0.436 |
MOD_ProDKin_1 | 1108 | 1114 | PF00069 | 0.632 |
MOD_ProDKin_1 | 1124 | 1130 | PF00069 | 0.488 |
MOD_ProDKin_1 | 1224 | 1230 | PF00069 | 0.670 |
MOD_ProDKin_1 | 1294 | 1300 | PF00069 | 0.630 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.441 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.380 |
MOD_ProDKin_1 | 696 | 702 | PF00069 | 0.377 |
MOD_ProDKin_1 | 815 | 821 | PF00069 | 0.531 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.432 |
MOD_ProDKin_1 | 961 | 967 | PF00069 | 0.429 |
MOD_ProDKin_1 | 968 | 974 | PF00069 | 0.435 |
MOD_SUMO_rev_2 | 1242 | 1249 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 755 | 761 | PF00179 | 0.282 |
MOD_SUMO_rev_2 | 862 | 867 | PF00179 | 0.401 |
TRG_DiLeu_BaEn_1 | 1370 | 1375 | PF01217 | 0.564 |
TRG_DiLeu_BaEn_1 | 153 | 158 | PF01217 | 0.298 |
TRG_DiLeu_BaEn_2 | 662 | 668 | PF01217 | 0.287 |
TRG_DiLeu_BaLyEn_6 | 246 | 251 | PF01217 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 661 | 666 | PF01217 | 0.304 |
TRG_ENDOCYTIC_2 | 1001 | 1004 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 1341 | 1344 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 1395 | 1398 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 647 | 650 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 706 | 709 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 779 | 782 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 953 | 956 | PF00928 | 0.515 |
TRG_ER_diArg_1 | 1235 | 1237 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 976 | 979 | PF00400 | 0.509 |
TRG_NLS_MonoCore_2 | 1233 | 1238 | PF00514 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 1281 | 1285 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 725 | 729 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 933 | 938 | PF00026 | 0.289 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 40% | 100% |
A0A1X0P171 | Trypanosomatidae | 29% | 100% |
A0A3Q8IJB0 | Leishmania donovani | 26% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 26% | 100% |
A0A3S7WU91 | Leishmania donovani | 27% | 99% |
A0A3S7WU94 | Leishmania donovani | 27% | 100% |
A0A3S7WU95 | Leishmania donovani | 25% | 100% |
A0A3S7XB85 | Leishmania donovani | 70% | 100% |
A4H8U6 | Leishmania braziliensis | 27% | 100% |
A4H8V5 | Leishmania braziliensis | 29% | 100% |
A4H8V7 | Leishmania braziliensis | 30% | 100% |
A4H8V8 | Leishmania braziliensis | 27% | 100% |
A4HX84 | Leishmania infantum | 27% | 100% |
A4HX85 | Leishmania infantum | 26% | 100% |
A4HX87 | Leishmania infantum | 27% | 100% |
A4IDA6 | Leishmania infantum | 70% | 100% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AQY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q25263 | Leishmania donovani | 26% | 100% |
Q26721 | Trypanosoma brucei brucei | 30% | 100% |
Q27675 | Leishmania donovani | 27% | 100% |
Q4Q1A1 | Leishmania major | 69% | 100% |
Q4QEH9 | Leishmania major | 26% | 100% |
Q4QEI0 | Leishmania major | 26% | 100% |
Q4QEI1 | Leishmania major | 26% | 100% |
Q4QEI2 | Leishmania major | 28% | 100% |
Q4QEI3 | Leishmania major | 27% | 100% |
Q99279 | Trypanosoma brucei brucei | 28% | 100% |
Q99280 | Trypanosoma brucei brucei | 30% | 100% |
V5AYH7 | Trypanosoma cruzi | 31% | 100% |